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The lysosomal trafficking regulator "LYST": an 80-year traffic jam.

Authors :
Turner ME
Che J
Mirhaidari GJM
Kennedy CC
Blum KM
Rajesh S
Zbinden JC
Breuer CK
Best CA
Barker JC
Source :
Frontiers in immunology [Front Immunol] 2024 May 07; Vol. 15, pp. 1404846. Date of Electronic Publication: 2024 May 07 (Print Publication: 2024).
Publication Year :
2024

Abstract

Lysosomes and lysosome related organelles (LROs) are dynamic organelles at the intersection of various pathways involved in maintaining cellular hemostasis and regulating cellular functions. Vesicle trafficking of lysosomes and LROs are critical to maintain their functions. The lysosomal trafficking regulator (LYST) is an elusive protein important for the regulation of membrane dynamics and intracellular trafficking of lysosomes and LROs. Mutations to the LYST gene result in Chédiak-Higashi syndrome, an autosomal recessive immunodeficiency characterized by defective granule exocytosis, cytotoxicity, etc. Despite eight decades passing since its initial discovery, a comprehensive understanding of LYST's function in cellular biology remains unresolved. Accumulating evidence suggests that dysregulation of LYST function also manifests in other disease states. Here, we review the available literature to consolidate available scientific endeavors in relation to LYST and discuss its relevance for immunomodulatory therapies, regenerative medicine and cancer applications.<br />Competing Interests: ChB and CaB are co-founders of Lyst Therapeutics, LLC Columbus, OH and did not receive support for the present work. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2024 Turner, Che, Mirhaidari, Kennedy, Blum, Rajesh, Zbinden, Breuer, Best and Barker.)

Details

Language :
English
ISSN :
1664-3224
Volume :
15
Database :
MEDLINE
Journal :
Frontiers in immunology
Publication Type :
Academic Journal
Accession number :
38774881
Full Text :
https://doi.org/10.3389/fimmu.2024.1404846